Characterization of alternatively spliced transcript variants of glycophorin A and glycophorin B genes in Chinese blood donors

• Published in: Vox sanguinis 2022-05, Vol.117 (5), p.715-723
• Main Authors: Liang, Yanlian, Ren, Jianwei, Zhong, Fuling, Hong, Wenxu, Su, Yuqing, Wu, Fan, Liang, Shuang, Liu, Jun, Fang, Shuanghua, Liang, Yanwen, Fan, Xiuchu, Lin, Jiansuo, Liu, Yi, Feng, Bo, Xu, Yunping
• Format: Article
• Language: English
• Subjects: alternative RNA splicing; Alternative Splicing; Amino acids; antigenic diversity; Antigens; Blood & organ donations; Blood Donors; Blood groups; Cell surface; China; Deoxyribonucleic acid; DNA; Fusion protein; Gene sequencing; Genes; Genotyping; Glycophorin B; Glycophorins - genetics; Glycophorins - metabolism; GYPA mRNA; GYPB mRNA; Humans; Hybrids; Insertion; MNS blood group system; MNSs Blood-Group System; Peripheral blood; Phenotyping; Polymerase chain reaction; Proteins; Ribonucleic acid; RNA; RNA, Messenger - blood; RNA, Messenger - genetics
• ISSN: 0042-9007; 1423-0410
• DOI: 10.1111/vox.13252

Background and Objectives The molecular basis of MNS blood group variants is not fully clear yet. In this study, we have characterized mRNA variants of GYPA and GYPB genes to reveal whether alternative RNA splicing may cause antigenic diversity of the MNS system. Materials and Methods Total RNA was extracted from peripheral blood of Chinese blood donors and full‐length cDNA products were generated. A nested polymerase chain reaction (PCR)‐based method was established for fragment amplification and Sanger sequencing. Resulted full‐length mRNA sequences were aligned with GYPA or GYPB genomic sequences respectively for exon identification. Amino acid (AA) sequences of GPA and GPB proteins were extrapolated and GYPA‐EGFP, GYPB‐EGFP fusion genes were generated to monitor subcellular distribution of the encoded glycophorin (GP) proteins. Results Totally 10 blood samples were analysed. GYPB mRNAs of all the subjects demonstrated frequent exon insertion or deletion whereas this kind of variation was only observed in 3 of 10 GYPA mRNA samples. None of the reported Miltenberger hybrids was detected in any of the mRNA samples. The alternative splicing resulted in changes of AA sequences in N‐terminal domains where the MNS antigenic motifs resided; however, subcellular localizations of GP‐EGFP fusion proteins showed that the above‐mentioned AA changes did not affect cell surface distribution of the encoded GP proteins. Conclusions Alternative RNA splicing may influence the antigenic features of GP proteins but not their cell surface distribution. Therefore, GYPA and GYPB mRNA characterization might be an invaluable supplement to serological phenotyping and DNA‐based genotyping in MNS blood grouping.